510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K971328Substantially Equivalent

Olympus Cd-6C-1 Coagulation Electrode

OLYMPUS Corporation of the Americas, Melville NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K971328 is the FDA 510(k) clearance record for OLYMPUS CD-6C-1 COAGULATION ELECTRODE, a class II device, cleared for Olympus America, Inc. on under FDA product code FFE (System, Water Jet Catheter, Renal). FDA records list 150 510(k) clearances for OLYMPUS Corporation of the Americas, from to . As of , FDA records show no recalls naming K971328.

Clearance record

Decision date
Received
(82 days to decision)
Product code
FFE System, Water Jet Catheter, Renal
Regulation
21 CFR 876.4650
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Olympus America, Inc. Two Corporate Center Dr., Melville NY
510(k) summary
Statement
Third party review
No

Clearances, product code FFE

Trailing 12 months

FDA records hold no clearances under product code FFE in the trailing twelve months.

FDA records show no clearances under product code FFE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FFE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260